Arecoline hydrobromide - ≥98% , CAS No.300-08-3

CAS: 300-08-3 Cat. No.: A107393 Peso molecular: 236.11 Beilstein Registry Number: 3914826 Número EC: 206-087-3
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Areciline Hydrochloride,(S) | Nicotinic acid,2,5,6-tetrahydro-1-methyl-, methyl ester, hydrobromide | s2614 | SR-01000075307-1 | NCGC00093563-04 | UNII-24S79B9CX7 | BCP02923 | BCP9000314 | Q27253878 | NCGC00093563-03 | NICOTINIC ACID, 1,2,5,6-TETRAHYDRO-1
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
A107393-1g
5
15,90US$
5g
A107393-5g
5
49,90US$
25g
A107393-25g
7
97,90US$
100g
A107393-100g
2
379,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Areciline Hydrochloride, (S) | Nicotinic acid, 2, 5, 6-tetrahydro-1-methyl-, methyl ester, hydrobromide | s2614 | SR-01000075307-1 | NCGC00093563-04 | UNII-24S79B9CX7 | BCP02923 | BCP9000314 | Q27253878 | NCGC00093563-03 | NICOTINIC ACID, 1, 2, 5, 6-TETRAHYDRO-1
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Muscarinic receptor agonist (EC 50 values are 7 (M 1 ), 95 (M 2 ), 11 (M 3 ), 410 (M 4 ) and 69 nM (M 5 )). Natural alkaloid. Induces decreased blood-brain barrier permeability.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488180964
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180964
Sonrisas canónicasCN1CCC=C(C1)C(=O)OC.Br
IUPAC Namemethyl 1-methyl-3,6-dihydro-2H-pyridine-5-carboxylate;hydrobromide
InChIKeyAXOJRQLKMVSHHZ-UHFFFAOYSA-N
INCHI1S/C8H13NO2.BrH/c1-9-5-3-4-7(6-9)8(10)11-2;/h4H,3,5-6H2,1-2H3;1H
Isómeros SMILES CN1CCC=C(C1)C(=O)OC.Br
WGK Alemania 3
RTECS QT2275000
Peso molecular 236.11
Beilstein 3914826
Reaxy-Rn 3914826
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3914826&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassAlkaloids and derivatives
ClaseNot available
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentAlkaloids and derivatives
Alternative Parents Hydropyridines  Methyl esters  Enoate esters  Trialkylamines  Amino acids and derivatives  Monocarboxylic acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Hydrobromides  Carbonyl compounds  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Alkaloid or derivatives - Hydropyridine - Methyl ester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Carboxylic acid ester - Amino acid or derivatives - Tertiary amine - Tertiary aliphatic amine - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Amine - Organic nitrogen compound - Hydrobromide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as alkaloids and derivatives. These are naturally occurring chemical compounds that contain mostly basic nitrogen atoms. This group also includes some related compounds with neutral and even weakly acidic properties. Also some synthetic compounds of similar structure are attributed to alkaloids. In addition to carbon, hydrogen and nitrogen, alkaloids may also contain oxygen, sulfur and more rarely other elements such as chlorine, bromine, and phosphorus.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EDNRA Tclin Endothelin receptor ET-A (5008 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCOLN3 Tchem MCOLN3 protein (319 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
nompc Ion channel NompC (277 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpc4 Short transient receptor potential channel 4 (1615 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

20 results found

Lot NumberCertificate TypeFechaArticulo
G2410602Certificate of AnalysisApr 03, 2026 A107393
G2410068Certificate of AnalysisApr 03, 2026 A107393
F2421100Certificate of AnalysisMar 17, 2026 A107393
J2028202Certificate of AnalysisFeb 05, 2026 A107393
F2213155Certificate of AnalysisDec 09, 2025 A107393
F2213157Certificate of AnalysisDec 09, 2025 A107393
F2213175Certificate of AnalysisDec 09, 2025 A107393
F2213176Certificate of AnalysisDec 09, 2025 A107393
L2419166Certificate of AnalysisDec 27, 2024 A107393
L2419150Certificate of AnalysisDec 27, 2024 A107393
L2419151Certificate of AnalysisDec 26, 2024 A107393
D1809093Certificate of AnalysisJul 17, 2023 A107393
D1809092Certificate of AnalysisJul 17, 2023 A107393
I2110046Certificate of AnalysisJun 09, 2023 A107393
I2110045Certificate of AnalysisJun 09, 2023 A107393
I2110041Certificate of AnalysisJun 09, 2023 A107393
B2324081Certificate of AnalysisMar 01, 2023 A107393
J2028204Certificate of AnalysisAug 11, 2022 A107393
E2311130Certificate of AnalysisSep 15, 2021 A107393
E2311126Certificate of AnalysisSep 15, 2021 A107393

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Propiedades químicas y físicas
Punto de fusión (°C)171-175°C
Peso molecular236.110 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass235.021 Da
Monoisotopic Mass235.021 Da
Topological Polar Surface Area29.500 Ų
Heavy Atom Count12
Formal Charge0
Complexity187.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
Referencias
1. Xiao Run-mei, Wang Jun-jun, Chen Jing-ya, Sun Li-juan, Chen Yong.  (2014)  Effects of arecoline on hepatic cytochrome P450 activity and oxidative stress.  JOURNAL OF TOXICOLOGICAL SCIENCES,  39  (4): (609-614).  [PMID:25056785] [10.2131/jts.39.609]
2. Jin Liu, Li Ma, Senwen Deng, Xinzhi Chen, Qi Li, Aiqing Xu, Ting Tong, Shuhua Tan, Mingkang Wang, Jiangtao Cai, Haihua Wang.  (2024)  Deep Eutectic Solvents for Efficient and Selective Extraction of α-Glucosidase Inhibitors from Waste Seeds of Refined Betel Nuts.  Foods,  13  (7): (1070).  [PMID:38611374] [10.3390/foods13071070]
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